FDA recall record

Scynexis BREXAFEMME (Ibrexafungerp) tablets 150 mg, 4 count cartons recall — FDA D-0042-2024

Cross Contamination with Other Products: Potential cross-contamination of ibrexafungerp citrate drug substance with ezetimibe (a non-antibacterial…

Class Iclassification
D-0042-2024official record ID
Oct 18, 2023report date

Recall record at a glance

Official recordD-0042-2024
CategoryDrug Recalls
ClassificationClass I
FDA record statusCompleted
Recalling firmScynexis, Inc.
Report dateOct 18, 2023
Recall initiation dateSep 25, 2023
Quantity17,376
LocationJersey City, NJ, United States

Official product description

BREXAFEMME (Ibrexafungerp) tablets 150 mg, 4 count cartons, Rx Only, Manufactured for and distributed by SCYNEXIS, Inc., Jersey City, NJ 07302 NDC 75788-115-04

Why the product was recalled

Cross Contamination with Other Products: Potential cross-contamination of ibrexafungerp citrate drug substance with ezetimibe (a non-antibacterial beta-lactam compound).

Distribution information

Nationwide in the US.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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